Novel polymerization initiator and process for polymerization using the same

ABSTRACT

A process for the polymerization of an olefinic monomer by contacting the monomer with a polymerization initiator having an oxidizing agent, a chelating compound of the metal, in which the metal is still capable of accepting one or more electron pairs from an electron donor and an electron donor in an amount at least equal to that required to complex completely the metal of the chelate compound. With the polymerization initiator, polymerization of the olefinic monomer can be accomplished at low temperatures employing oxidizing agents which are stable at the lower temperatures. Also, the solubility of the initiators allows polymerization by suspension process.

- United States Patent Chabert et al.

[451 Jan. 14,1975

NOVEL POLYMERIZATION INITIATOR AND PROCESS FOR POLYMERIZATION USING THE SAME Inventors: Henri Chabert, Chapurlat; Robert Aime, Lyon; Claude Gigiou,

Vernaison; Michel Ruaud, Villeneuve Par Ternay, all of France Assignee: Rhone-Poulenc S.A., Paris, France Filed: June 19, 1970 Appl. No.: 63,999

Related U.S. Application Data Continuation of Ser. No. 637,356, May 10, 1967, abandoned.

Foreign Application Priority Data May 13, 1966 France 66.61596 [58] Field of Search 260/85.5 R, 85.5 M, 949C, 260/887, 92.8, 89.1, 87.5, 88.1, 85.7

[56] References Cited UNITED STATES PATENTS 9/1952 Vandenberg 260/887 Primary Examinerl-Iarry Wong, Jr. Attorney, Agent, or FirmCushman, Darby & Cushman [57] ABSTRACT A process for the polymerization of an olefinic monomer by contacting the monomer with a polymerization initiator having an-oxidizing agent, a chelating compound of the metal, in which the metal is still capable of accepting one or more electron pairs from an electron donor and an electron donor in an amount at least equal to that required to complex completely the metal of the chelate compound. With the polymerization initiator, polymerization of the olefinic monomer can be accomplished at low temperatures employing oxidizing agents which are stable at the lower temperatures. Also, the solubility of the initiators allows polymerization by suspension process.

5 Claims, N0 Drawings NOVEL-POLYMERIZATION INITIATOR AND PROCESS FOR POLYMERIZATION USING THE SAME I This is a continuation, of application Ser. No. 637,356, filed May 10, 1967, and now abandoned.

This invention relates to the polymerisation of olefinic monomers, and to polymerisation initiators for use in such polymerisation.

Many polymerisation initiating systems of the free radical type, known as redox systems, which consist of a combination of an oxidising compound and a reducing compound, have been proposed. The oxidising compound of these systems is generally either a compound containing a mineral ion, such as the persulphate or chlorate ion, hydrogen peroxide, or an organic peroxide. The reducing compound may be a compound containing a reducing anion such as the bisulphite anion, or a metal compound in which the metal is in a lower state of oxidation, e g., Fe, or an organic reducing compound such as benzoin, ascorbic acid, dihydroxyacetone, an amine, preferably a tertiary amine having the most pronounced reducing properties, or a sugarv Such systems are described in HoubenWeyl Methoden der Organischen Chemie Makromolekulare Stoffe 14/1, pp. 263 to 297. Ternary systems consisting of redox systems of this general kind and small quantities of compounds providing metallic ions, which act as activators, have also been proposed. For these systems, the redox systems have generally consisted of oxidising agents such as organic persulphates or peroxides, and reducing agents such as benzoin, dihydroxyacetone, a bisulphite acetaldehyde addition compound, acetoin, benzenesulphinic acid, or triethanolamine, employed in approximately equal molecular quantities. The activators havebeen, more particularly, salts of chelates of metals such as iron, lead, nickel, cobalt, manganese or zinc, more particular naphthenates, stearates, oleates, cyclohexanecarboxylates and acetylacetonates (cf. W. Kern, Makromol. Chemie l, 249 to 268 (1947)). These ternary systems, which have been employed for bulk polymerisations, have a high mole ratio of reducing agent to metallic compound, which may be as great as 40:1 to 120:1.

The present invention provides a new polymerisation initiator comprising, in combination, (1) an oxidizing agent, (2) a chelate compound of a metal of Group 18, 118, NE, VB, V113, V118, 111A, IVA, VA, or VIII of the Periodic Table with an at least bidentate ligand, in which compound the metal is still capable of accepting one or more electron pairs from an electron donor, and (3) and electron donor in amount at most equal to that required to complex completely the metal of the chelate compound. Components (2) and (3) may be present in the initiator in the form of a preformed complex.

The three components of the new intitiators are, in more detail, as follows: l. Oxidising agents Suitable oxidising agents for use in the new initiators include: inorganic oxidising agents such as hydrogen peroxide, persulphates, permanganates, chlorates, perchlorates, bichromates, bromates and ceric (Ce salts; and organic oxidising agents such as oxaziranes (e.g., 2-butyl-3-isopropyl-oxazirane), and organic peroxides and hydroperoxides, including, more particularly, the acyl peroxides, for example, acetyl, benzoyl, lauroyl, terephthaloyl, and acetyl-lauroyl peroxides,

the alkyl, cycloalkyl, and aryl peroxides, for example, t-butyl, lauryl, t-butyllauryl, cyclohexyl and cumyl peroxides, and the hydroperoxides, forexample cyclohexyl and cumyl hydroperoxide.

2. Chelate compounds The chelate compounds used in the new initiators have a central metallic atom which still possesses the ability to accept at leat one electron doublet from an electron donor atom, i.e., the degree of co-ordination of the central metallic atom is lower than the maximum degree of co-ordination of this atom.

The co-ordination number of a metallic acceptor atom represents the number of atoms directly attahced to this central atom in a complex. With some metals in a high degree of oxidation, this co-ordination number is fixed and is characteristic of the metal, without the co-ordination number and the degree of oxidation being the same; while with other metals the coordination number may have various different values for a given degree of oxidation. ln some cases, a correlation may exist between the co-ordination number and the degree of oxidation, while in other cases the coordination number is the same regardless of the degree of oxdiation. The co-ordination number sometimes depends upon the nature of the donor atom.

The chelates employed in the present invention may be represented by the general formula:

in which M represents a metal atom of group IB, llB,

IVB, VB, VlB, VllB, lllA, lVA, VA or VIII of the Periodic Table (see, e.g., Handbook of Chemistry and Physics, 45th Edition, p. 8.2), preferably titanium, iron, vanadium, aluminium, tin, manganese, chromium,

cobalt, copper, zinc, or bismuth; D represents an electron-doublet donor group such as one of these defined by Dwyer and Mellor in Chelating Agents and Metal Chelates, 1964, pp. 17 and 18; A is an organic residue carrying the groups D and consisting of a hydrocarbon chain optionally substituted by groups which are not electrondoublet donors, or of a substituted or unsubstituted, aliphatic or aromatic, cyclic or polycyclic,hydrocarbon residue, or of both of a hydrocarbon chain and a cyclic residue; X represents either an anion, such as a halide, sulphate or nitrate anion, or a cation, such as an alkali metal (e.g., Na*, K*, or Li ammonium or quternary ammonium cation; Q represents an oxygen or sulphur atom or an organic radical such as a lower alkyl, cycloalkyl, aryl, lower alkoxy, cycloalkoxy radical; p is an integer equal to or higher than 2, which represents the number of donor groups in the ligand of formula D A; s is nought or an integer, and m is an integer equal to or higher than 1, s and m being such that (pm s) has a value lower than the maximum coordination number of the metal M; and n is nought (in the case of non-ionisable chelates) or an integer or an improper fraction (in the case of ionisable chelates) corresponding to the number of electrical charges of the grouping [MQR(D,,A),,,], which is then a chelate ion.

Although chelates in which the ligand of formula' D A is tri-, quadri or quinque-dentate may be employed in the initiator of the present invention, it is preferably to employ chelates in which the ligand or ligands are bidentate. A list of such ligands is given by Dwyer and Mellor loc. cit., pp. 95-132. Suitable such bidentate ligands include: diacids such as oxalic acid, malonic acid or l-carboxyphenylacetic acid; hydroxy acids such as glycollic acid, lactic acid and salicyclic acid; o-diphenols such as catechol; hydroxyaldehydes such as o-hydroxybenzaldehyde (salicylaldehyde); hydroxy ketones such as o-hydroxyacetophenone; diols such as ethylene gylcol; diamin es such as ethylene diamine, 1,3-diamine-propane, u-phenylcne-diamine, l-phenylcthylcnc-l,Z-diaminc; his-hetcrocyclic compounds such as 2,2-bipyridyl and l,l()-phenanthroline; amino acids such as glycine, anthranilic acid, aand B-aminobutyric acids, 2-pyrrolidine-carboxylic acid (proline), l-amino-cyclopentan e-carboxylic acid; aminophenols such as aminophenol; hydroxylated heterocyclic compounds such as 8-hydroxy-quinoline; hydroxyaldimines such as benzaldimine; thioalcohols such as 2-mercaptoethanol; and thioacids such as thioglycollic acid. A preferred class of bidentate ligands consists of the ,B-dicarbonyl compounds of the general formula:

n-c-cH-c-R' in which R represents a hydrogen atom or a substituted or unsubstituted hydrocarbon radical, or an alkoxy radical, R represents a substituted or unsubstituted hydrocarbon radical, it being possible for R and R to be identical when they both represent hydrocarbon radicals, and R" represents a substituted or unsubstituted hydrocarbon radical, or a hydrogen or chlorine atom. More specifically, the hydrocarbon radicals which may be represented by R and R include alkyl radicals, such as methyl, ethyl, propyl, butyl and octyl, cycloalkyl radicals, such as cyclopentyl and cyclo-hexyl, aryl radicals, such as phenyl and naphthyl, aralkyl radicals such as benzyl, substituted alkyl radicals such as trifluoromethyl, alkoxyalkyl radicals such as ethoxymethyl; and substituted aryl radicals such as o-methoxyphenyl, 2,3- dichlorophenyl and 4-hydroxyphenyl..

The alkoxy radicals which may be represented by R include more particularly metnoxy, ethoxy, propoxy and butoxy. The hydrocarbon radicals which may be represented by R" include more particularly lower alkyl radicals such as methyl, ethyl, propyl and butyl.

Two of the symbols R, R and R may also represent in combination a divalent hydrocarbon chain (for example polymethylene), the rings which they then form with the remainder of the molecule then containing five or six carbon atoms.

The dicarbonyl compound is formula II may also be a bicyclic compound in which the group is common to both rings.

Examples of the compound of formula II are: diketones such as acetylacetone (2,4-pentanedione), 2,4 hexanedione, 2,4-heptanedione, 5-methyl-2,4- hexanedione, 2,4-octanedione, 3-methoxy-2,4- petanedione, 3,5-hep'tanedione, l,l,l-trifluoro-2,4- pentanedione, benzoylacetone, dibenzoylmethane', o-methoxybenzoylacetone, l,l ,l-trifluoro-2- N-phenyl-0-hydroxy-' benzoylacetone, B-naphthoyl-trifluoroacetone, 3-methyl-2,4-pentanedione, 3-butyl-2.4-pentanedione, l,3-cyclopentanedione, 1,3-cyclohexanedione, 5,5- dimethyl-l,3-cyclohexanedione (dimedone), 2-acetylcyclohexanone, l,8-hexahydronaphthalenedione, and l-hydroxy-benzoylacetone;

B-keto-aldehydes such as propionylacetaldehyde, benzoylacetaldehyde, and a-formylcyclohexanone; esters of a-keto-acids such as methyl, ethyl and butyl acetoacetate, and methyl benzoylacetate.

Examples of bidentate chelate compounds which may be used in the invention are: ferrous acetylacetonate, vanadyl acetylacetonate, vanadyl methylacetylacetonate, vanadyl 2-acetylcyclohexanate, vanadyl heptanedionate, vanadyl propionylacetaldehydate, vanadyl benzoylacetaldehydate, dichlorotitanium acetylacetonate, diethyl-tin acetylacetonate, cupric acetylacetonate, vanadyl salicylaldehydate, vanadylbis(acetylacetamide), vanadyl-bis(acetylacetanilide), vanadyl thioglycollate, vanadyl anthranilate, ethoxyaluminium acetylacetonate, and vanadyl a-formylcyclohexanonate.

Examples of tridentate ligands are 2,6-bis(apyridyl)pyridine and 2-(oz-pyridylmethyleneaminomethyl)pyridine, and, of tetradentate ligands, bisbenzoylacetonepropylenediimine.

3. Electron donors Generally speaking, the electron donor must be a unidentate ligand producing co-ordination by a o' electron doublet. However, if, because of its degree of coordination in the chelate compound (2), the metal can only accept one further electron doublet, this new doublet may be supplied by a ligand comprising two or more doublet-donor groups. Generally speaking, the electron donor compound may comprise as the donor group one of those mentioned for the ligands of the chelate compound. Thus, it is possible to employ monoamines such as methylamine, ethylamine, nbutylamine, cyclohexylamine, or diphenylamine; monoalcohols such as methanol, ethanol, propanol, butanol, cyclohexanol or benzyl alcohol; ethers such as dimethyl ether, diethyl ether, dibutyl ether, methyl cyclohexyl ether, methyl phenyl ether, dioxan, and tetrahydrofuran; aldehydes such as formaldehyde, acetaldehyde or benzaldehyde; imines such as acetaldimine; hydroxylamine and its derivatives, such as cyclohexyloxime or benzaldoxime; ketones such as acetone, or

methyl ethyl ketone; amides such as acetamide, propionamide, formamide or urea; or sulphur derivatives such as sulphonamides or phosphorus derivatives such as hexamethylphosphotriamide.

Although any compound comprising a doublet-donor atom may be employed, the best results are obtained with compounds whose reducing character is least pronounced, unlike what happens with the previously known ternary redox systems mentioned above. Thus, for a given monomer, the polymer yield is higher with primary amines than with tertiary amines.

As already mentioned the chelate compound (2) an the electron donor (3) may be separately added -to the new polymerisation initiator to form a complex in situ, or this chelate/donor complex may be preformed and introduced as such into the initiator combination.

The new initiator is suitable for the polymerisation of olefinic monomers comprising at least one olefinic double bond, and more especially of monomers in which the olefinic double bond is in the a,B-position to an activating grouping. The various monomers which may be polymerised may be represented by the formula:

III R2 u in which R R R and R each represent a hydrogen atom, a halogen atom, a functional grouping, or a substituted or unsubstituted hydrocarbon radical. More particularly, R R R and R may be chlorine, bromine or fluorine atoms or alkyl, cycloalkyl or aryl radicals, or heterocyclic radicals, or alkoxy, carboxy, alkoxycarbonyl, aryloxycarbonyl, carbamoyl, nitrile, acyl, alkylthio, alkylsulphonyl, arylsulphonyl, aldehyde, alkylcarbonyloxy or arylcarbonyloxy groups.

Suitable monomers include: vinyl chloride, vinylidene chloride, vinyl and allyl esters such as vinyl acetate, propionate and benzoate; acrylic and methacrylic acids and their derivatives such as alkyl acrylates, acrylamide, acrylonitrile, and ethylene-glycol diacrylates; vinyl ketones such as 3-butene-2-one; vinyl ethers such as vinyl ethyl ether; unsaturated aldehydes such as acrolein; vinyl sulphones such as vinylphenylsulphone;

heterocyclic compounds substituted by a vinyl group such as vinylpyridines and vinylpyrrolidones; vinyl thioethers such as vinyl ethyl sulphide; and purely hydrocarbon compounds such as divinylbenzene and ethylene. These compounds may be homopolymerised or copolymerised with one another or with copolymerisable resins such as unsaturated polyesters.

The new initiating system may be employed in all modes of polymerisation: in bulk, in solution, in emulsion or in suspension. It is particularly suitable for this last mode of polymerisation, in which use must be made of oil-soluble initiators. In this case, the oxidising agent is preferably an organic peroxide or hydroperoxide, the chelate compound, achelate of a B-dicarbonyl compound, and the electron donor a compound which is only partially soluble in the monomer.

The temperature at which the polymerisation is carries out may vary from to +l00C, depending upon the initiating system and the monomer employed. Because of their high activity, the new initiating systems make it possible to carry out polymerisations at elevated temperature, i.e., at temperatures above 30C, employing only extremely small quantities of initiator. It is thus possible to obtain polymers comprising very few initiator residues, and this constitutes an important advantage of the new system over previously known systems. At low temperatures, the new initiators show an activity which is not shared by any of the various constituents taken individually or in pairs.

The quantities of oxidising agent and chelate compound may vary within fairly wide limits. In general, they maybe used, in each case, in a molar proportion of 0.0005 percent to 5 percent based on the monomer, although molar proportions from 0.0005 percent to 0.1 percent are generally sufficient. In addition, the molar proportion of chelate compound may generally be lower than the molar proportion of oxidising agent. The quantity of electron donor employed must be, as already stated, at most equal to that which the metal of the chelate is still capable of complexing. When the polymerisation in question is a bulk polymerisation with an electron donor which is soluble in the monomer, or a solution polymerisation in an organic solvent, or a polymerisation in a heterogeneous medium-with'an electron donor which is soluble only in the monomer, the quantity of electron donor to be added to the reaction medium is at most equal to that which the metal of the chelate is still capable ofcomplexing. On the otherhand, in the case of a polymerisation in a heterogeneous medium with an electron donor which is partially soluble in the phase which does not contain the monomer, the quantity of electron donor to be added may be greater than that which the metal of the chelate is still capable of complexing, so that, taking into account the partition coefficient between the phases, the initiating system present in the phase containing the monomer satisfies the aforesaid condition. In all cases, the quantity of electron donor to be actually added may be readily determined by a simple preliminary test, the polymerisation reaction being inhibited when the quantity of electron donor present in the monomer is greater than that which the metal of the chelate present in this same monomer can complex.

Polymerisations using the new initiators may be carried out in the presence of the usual polymerisation ad'- juvants; e.g., emulsifiers, suspending agents, and antigels (in the case of low-temperature polymerisations). When the electron donor is alkaline, as is the case with ammonia and the amines, it is preferable, if the monomer is likely to undergo an alkaline hydrolysis, to carry out the operation in the presence of a buffer such as, for example, sodium bicarbonate.

In the case of solution polymerisation, the same organic solvents may be employed as in known processes, However, when the solvent employed is an electron donor (e.g., an alcohol or amide such as dimethylformamide), it is necessary to choose as electron donor in the initiating system a compound which gives with the chelate compound employed a complex which is more stable than that formed with the solvent, i.e., the donor chosen must be able to displace the solvent from the 7 complex which the latter may have formed with the chelate compound. However, it is preferable to employ a solvent which is not an electron donor, e.g., a saturated hydrocarbon such as hexane, heptane or cyclohexane. I The new initiators afford many advantages over previously known catalytic systems. In the first place, they make it possible to carry out polymerisations at low temperature employing as oxidising agents substances which, like lauroyl and benzoyl peroxides, are stable at ambient temperature, while the initiating systems used in earlier low temperature polymerisation processes necessitate the use of compounds which must decompose at sufficient speed at low temperature to initiate the polymerisation, and which consequently exhibit at ambient temperature an instability such that they are capable of causing explosions.

Another advantage of the new initiators resides in the possibility which they afford, because they involve the use of compounds which are soluble in the monomer, of performing low temperature polymerisations by the suspension polymerisation process. Suspension polymerisation in water of vinyl monomers such as vinyl chloride and vinyl acetate affords many advantages over emulsion polymerisation: the polymer is readily recoverable by filtration; in addition, the suspending agents employed for the suspension polymerisation (such as, for example, polyvinyl alcohol or polyvinylpyrrolidone) have the advantage that they may be eliminated by washing the polymer in water, or that they may optionally be left in the polymer without any major disadvantage, while on the other hand the emulsifiers employed in. emulsion polymerisation are difficult to eliminate and often catalyse the degradation of the polymer.

In the case of the polymerization of vinyl chloride, the new initiators also make it possible, without employing low temperatures, but simply operating at a temperature of 1020C, to obtain polymers which have thermomechanical properties (elongation, transition point, and Vicat point) similar to those of polymers obtained at lower temperatures with other initiating systems. In addition, a comparative study of the infra-red spectra shows that the polyvinyl chloride thus obtained has substantially the same structure as the polyvinyl chloride obtained by earlier processes at lower temperatures. The tacticity of polyvinyl chloride is assessed by the ratio D of the optical densities of the bands at 1,428 cm and at 1,434 cm of the infra-red spectrum of the polymer [see Germar, Makrom. Chem. 60, 106, (1963); and Takeda Polym. Sci., 57, 383 (1962)]. This ratio increase with the tacticity of the polymer. Vinyl-chloride polymers prepared at a temperature of 1020C with the new initiators have a ratio D similar to the ratio D of polymers obtained at temperatures below C with other initiators. which in dicates a similar tacticity in agreement with the similarity of the thermomechanical properties.

The new initiators also make it possible to polymerise a'olefines including more particularly ethylene, at low pressure. By low pressure is meant pressures between 1 and 100 bars absolute. Previously, the polymerisation of ethylene with free radical-type catalysts has involved the use of temperatures of 250C or more and pressures of at least 300 bars, generally 1,000 bars or more.

The following Examples illustrate the invention.

EXAMPLE 1 a. Into a l-litre glass autoclave equipped with a stirring system, a thermometer tube and a device for charging the reactants through a valve, 400 cc. of deionised water, 1 g. of polyvinyl alcohol having a saponification index of I25, 2 g. of lauroyl peroxide (5.025 X mol.), 0.650 g. of vanadyl acetylacetonate (2.453 X 103 mol.) and 0.200 g. of dilaurylamine (5.665 X 10 mol.) are introduced under nitrogen. Stirring is started, and, while the autoclave is maintained at a temperature of 16C by circulation of water through a double jacket surrounding the reactor, 100 g. of vinyl chloride (i.e., 1.6 mol.) are introduced. After reaction for 20 hours at 16C, the autoclave is degassed. The polymer is filtered off and washed with deionised water. After drying in vacuo, 60 g. of polyvinyl chloride (polymer I) are obtained. The viscosity index of a solution having a concentration of 5 g/l. in cyclohexanone at C is 282 cm /g. The degree of conversion is 60 percent.

b. The same procedure is followed as in part (a), but with the following initiator: lauroyl peroxide (2.5 X

10 mol.), vanadyl acetylacetonate (6.3 X 10 mol.), 6

c Another polymer is prepared (polymer III) by polymerisation of vinyl chloride at 10C in suspension in the presence of tichloroacetyl peroxide. A product having a viscosity index of 325 em /g. is obtained.

d. Another polyvinyl chloride (polymer IV) is prepared by polymerisation at 60C in the presence oflauroyl peroxide. This polymer has a viscosity index of 100 cm /g.

These polymers are examined by infra-red spectrography, and for each the ratio D of the optical densities at 1,428 cm and 1,434 cm is determined; this ratio expresses the degree of syndiotacticity of the polymers. In addition, the transition temperature, the Vicat point and the elongation at C under 50 kg/cm of the same polymers are determined. These results are all set out in the following Table:

Polymer Transition Vicat Elongation D point C point C 71 I 83.5 119 50 1.53 ll 83 134 50 1.48 111 85 123 22 1.50 IV 76.5 1.25

These results show the similarity of the properties of polymers I and II obtained at +16C by the new process with those of polymer III obtained at 10C by a known process. Polymer IV, prepared at 60C by a known process, is quite different.

EXAMPLE 2 The procedure of Example 1 is followed, with the fol- EXAMPLE 3 In the autoclave of Example 1, a series of polymerisation experiments as in Example 1 is performed, the dilaurylamine being replaced by diphenylamine and the quantities of vanadyl acetylacetonate and amine being varied as indicated in the following Table. which also gives the results obtained:

Experi- Lauroyl Vanadyl Diphenyl- Yield Viscosity ment peroxide acetylaceamine of index (moles) tonate (moles) poly- (em /g.)

mer (moles) 7r A 5 X 10 2.4 X 10 6.1SX1'0 70 257 B do. do. l.23 l0' 67 188 C do. 1.2 X 10 do. 50 156 D do. do. 492x10 31 insoluble.

CI'OSS- linked polymer These experiments show that an increase in the quantity of diphenylamine (i.e., electron donor) employed results, beyond certain values, in an appreciable lower- 9 10 ing of the yield and of the viscosity index, and may A series of comparative experiments is carried out as cause some cross-linking of the polymer. in Example 1, the polymerisation being effected at 16C for l9 hours employing polyvinylpyrrolidone hav- EXAMPLE 4 ing an index K 90 as suspending agent, and with the By the procedure of Example 1, the following com- 5 quantities of cumene hydroperoxide, vanadyl acetylacparative experiments are carried out: etonate and cyclohexylamine given in the following Ta- Experiment Temperature Lauroyl Vanadyl Ammonium Degree Viscosity of 'polymeriperoxide acetylhydroxide of conindex sation "C (moles) acetonate (moles) version (em /g.)

' (moles) A 23 1.25Xl' 1.2SXl0' none 1 B 40 do. do. none 5 81 C 40 dov none 6 102 D 40 do. l.2SXl0 10' 92 158 E 40 do. do. 10 89 l58 Experiments A, B and C show that in the absence eible, in which the results obtained are also set out:

ther of the electron donor or of the chelate compound, the degree of polymerisation is low, even when the temperature is increased. On the other hand, the addition Experi- Chutgjtene vamlldyl g clt Dfcgrce Viscosment y roacety aceexy 0 con ity of a small quantity of ammonia, of which only a small peroxide mime amine version index proportion 15 effective in the initiator because of its low (moles) (moles) (moles) (cm lg) ,brin s the de ree of the consoluinhty m the monomer g g A 125x10 125x10 2.5 i0- 40 225 version to 'P ,B x10 3.5 |0- none 24 94 C do. none do. 0

v EXAMPLE 5 30 A series of comparative experiments is carried out as Experiments A and B show that in the absence of the in Example 1, the polymerisation being effected for 20 electron donor, even when the peroxide/chelate system hours at 16C with the quantities of lauroyl peroxide, is increased by 2.25 l0 mol., the polymerisation vanadyl acetylacetonate and electron donor indicated yield falls (to 24 percent instead of 40 percent), and in the following Table, which. also gives the results obthat in addition an appreciable lowering of the viscosity tained. index of thepoly'mer occurs. The transition point is Experiment Lauroyl Vanadyl Electron Degree Viscosity peroxide acetylacedonorof conindex (moles) tonate (moles) version (em /g.) (moles) A 1.25 10- l.25 l0 n-butylamine 370 l.2Xl0

do. do. n-butylamine 45 1.2 10- C do. do. di(nbutyl)- 25 amine i.2 1o-= D do. do. tri(n-butyl)- 2 amine l.2xl0"= Because ofthe partition coefficient ofthis amine between the monomer and the aqueous phase. the molar proportion of amine to chelate in the monomer is in fact lower than ltl.

' Because of the partition coefficient of this amine be- 72.5C for the polymer of experiment B against C tween the monomer and the aqueous phase, the molar for the polymer of experiment A (a value similar to that proportion of amine to chelate in the monomer is in of the polymers l and ll of Example I). fact lower than lzl.

Experiments A, B, C, and D show that the degree of EXAMPLES 7 To 14 conversion fails when the primary amine is replaced by y he procedure Of Example I, u Series of experia secondary or tertiary amine, the reducing power of 65 ments is CaTfiedQul, the Polymerlsatlon being min" hi h increases i h h degree f b i i ued for 20 hours in each case at the temperature indicated in the Table the constituents of the initiating sys- EXAMPLE 6 g tent and the results being also given in the Table:

Example Polymeri- Lauroyl Chelate Electron Degree Viscosity sation peroxide (moles) donor ofcon- Index tempera- (moles) (moles) version .(cmlg) ture C 7 16 1.25X10 vanadyl monomethyl- 16 405 acetylaceamine* tonate 1.35X1O' (a) 1.25X10 8 10 do. do. do. 13 710 9 16 do. do triethyl- 36 384 amine* 8.9X10'(b) 10 do do. do diethyl- 43 I 382 amine* 125x10 11 10 X10 vanadyl diphenyl- 48 353 acetylaeeamine tonate 6.15X 2.4X10' 12 16 do vanadyl do. 76 256 methylacetylztcetonate 2.4X10"" it do. do vanudyl do. 30 150 Z-ucetyleyclohcxnnonutc 2.4 10

14 do. do vunztdyl do. 59 230 hcptuncdionate 2.4X10

' For these amines. the quantity of amine employed is not in fact that which acts in the initiator system. Sinee these amines are very soluble in water. only a part. that p ding l" l ility in v y chloride. is utilised in the initiator.

(a) Employed as a 30% weight-by-volume aqueous solution in a quantity of 1.4 cc (b) Employed as a 25% weight-hy-volumc aqueous solution in quantity 013.6 cc.

EXAMPLES 15 to 43 By the procedure of Example 1, a series of Examples is carried out, the constituents of the initiator and the results being as given in the following Table:

For these amines, the quantity of amine employed is not in fact that which acts in the initiator system. Since these amines are very soluble in water, only a part, that corresponding to the solubility in Degree of Polymerisation Electron Viscosity Example Duration temperature Oxidanttmoles) Chelate (moles) Donor Conversion index (hours) "C (moles) (em /g) 15 16 lauroyl peroxide vanadyl acetylacetonate N1-1.CH 97 296 2.5 X 10 2.4 X 10' 10 16 do. 40 do. do. do. 92 158 1.25 X 10 1.25 10' 10 17 do. 10 do. do. do. 20 740 2.5 X 10 6.3 X 10 10" 18 do. 16 do. do. do. 37 592 2.5 X 10 7.9 X 10 10 19 do. i 16 2,4 dichlorobenzoyl do. do. 79 391 peroxide 2 X 10 1.23 X 10' 10 20 26 16 cumene hydroperoxide do. do. 46 250 1.25 X10" 7 1.25 X10 2.2 X 10' 21 24 16 2,4-dichlorobenzoy1 vanadyl propionylacetal- NH CH 24 peroxide dehydrate 1.25 X 10 1.25 X 10" 2.2 X 10 v 22 do. do. do. vanadyl benzoylacetaldo. 19

' dehydrate 1.25 X 10 23 24 16 do. vanadyl propionylacetaldo. 24 V dehydrate 1.25 X 10 24 do. do. do. vanadyl benzoylacetaldo. 19

dehydrate v 1.25 X 10 25 22 16 do. dichlorotitanium acetyldo. 45

acetonate 1.25 X 10' 26 24 do. do. diethyl-tin acetyldo. 62

acetonate 4 1.25 X 10 27 22 16 2,4-dich1orobenzoy1 cupric acetylacetonate NH 0H peroxide 1.25 X 10 1.25 X 10 2.2 X 10 Polymerisation Electron Degree of Viscosity Example Duration temperature Oxidant (moles) Chelate (moles) Donor Conversion Index (hours) "C o es) (cmVg) 28 24 do. do. vanadyl salicyladehydrate do. 44

1.25 X 29 do. do. do. vanadyl bis(acetyldo. 29

acetamide) 1.25 X 10 30 do. do. do. vanadyl bis(acetyldo. 41

acetanilide) 1.25 X 10* 31 do. do. do. vanadyl thioglycolate do. 6

- 1.25 X 10" 32 do. do. do. vanadyl anthranilate do. 15

1.25 X 10 33 21 16 2,4-dichlorobenzoyl vanadyl acetylacetonate acetamide 61 peroxide 1.25 X 10' 1.25 X 10* 2.2 X10 34 do. do. do. do. diethyl 63 ether 1.15 X 10 35 do. do. do. do. dioxane 72 1.85 X 10 36 do. do. do. do. urea 70 2.1 X 10 37 do. do. do. zinc acetylacetonate diethyl 1 l ether l.25 lO l.l5 l0' 38 do. do. lauroyl peroxide vanadyl acetylacetaonate hydrazine 39 1.25 X 10' 1.25 X10 2.1 X10 39 22 17 2,4-dichlorobenzoyl ethoxyaluminium acetyl- Nl-1 OH 44 peroxide 7 acetonate 1.25 X 10' 1.25 X 10* 2.2 X 10 40 do. 16 di-(t-butyl) peroxide manganous acetyldo. 53

'acetonate 1.24 X10? 1.25 X 10 41 24 do. 2,4-dichlorobenzoyl titanyl acetylacetonate do. 63

peroxide 1.25 X 1O- 1.25 X 10 42 19 do. do. ethyl titanyl-bis(acetyldo. 12

' acetate 1.25x 10* 43 do. 15 3 isopropy1-3-butylvanadyl acetylacetonate do. 26

oxazirane EXAMPLE 44 EXAMPLE 46 A vanadyl acetylacetonate/butylamine complex is prepared by the method of Clauch et al., J. Amer. Chem. Soc. 83, 1073 (1961), from 0.01 mol. of the chelate and 0.01 mol. of the amine. A maroon-green crystalline product is obtained in a yield of 60 percent, which is identified by analysis and ultra-violet spectrography as the complex of the formula:

Vinyl chloride is polymerised in the autoclave employed in Example 1 atl6C for 18 hours using the following starting materials: water (400 cc.), vinyl chloride (100 g.). polyvinylpyrrolidone (l g.). 2,4- dichlorobenzoyl peroxide (1.25 X 10 mol.) and of conversion into polymer amounts to 80 percent.

EXAMPLE lnto the apparatus described in Example 1, distilled water (400 cc.). polyvinylpyrrolidone having an index k X 90 (l g.). ammonium .persulphatc (1:25 10"" mol.), vanadyl acetylacctonatc (1.25 X 10"mo1.), and ammonia (2.2 X 10" mol. in the form of an aqueous 'solution having a density of 0.900) are introduced.

After reaction for 19 hours at 16C, the degree of conversion is 73 percent into a polymer partially soluble in cyclohexanone.

An emulsion polymerisation is carried out by replacing the polyvinylpyrrolidone of Example 45 by sodium dodecylbenzenesulphonate (0.8 g.) as emulsifier. The other materials introduced into the autoclave are water (400cc.), vinyl chloride (100 g.), KBrO (2.5 X 10" mol.), vanadyl acetylacetonate (1.25 X 10 mol.), diethyl ether (1.15 X 10 mol.), and NaHCO (1.6 g.), as buffering agent for the medium. In 20 hours at 16C, a polymer having a viscosity of 285 cc/g. is obtained with a degree of conversion of 94 percent.

EXAMPLE 47 EXAMPLES 48 TO 51 A series of Examples of the solution polymerisation of vinyl chloride (1.6 mol'.) is carried out under the conditions given in the following Table with the results shown.

Example Duration Polymerisution Oxidunt Solvent Chelute Electron Degree of (hours temperature C (moles) (cm) (moles) donor conversion (moles) 71' 48 18 16 potassium methanol vanudyl cyclo- 20 bromate 300 acetylacehexylamine 2.5 X-= tonnte 25x10 2.5 1O 49 19 16 lauroyl hexane vanadyl do. 43

peroxide 200 3-chloro- 2.5)(10 acetylacetonate 2.5 10 50 2 2O do. methanol vanadyl isopropyl- 27 300 acetylaceamine tonate 2.S 1O' 25x10 51 3 16 do methanol do. NH OH 42 EXAMPLE 52 off, washed on the filter with distilled water, and dried Into a SOO-cc. round-bottomed flask provided with a stirring system, a nitrogen supply duct and a thermometer tube and immersed in a bath maintained at C, vinyl acetate (100 g., 1.162 mol.), water (200 cc.), and polyvinylpyrrolidone (1 g.) are introduced. After purging the flask with nitrogen, an initiating system comprising 2,4-dichlorobenzoyl peroxide (2.5 X 10 mol.), vanadyl acetylacetonate (2.5 X 10 mol.), and ammonia (1.1 X 10" mol.) is added. After 21 hours at 15C, the reaction is stopped, and the polymer is then filtered in vacuo. g. of polymer having a viscosity index of 47 cm /g.'(measured on an 0.5 percent solution in cyclohexanone) are obtained.

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Example Monomers Polymerisation Pressure Duration Reaction Emulsifier suspending temperature C (bars) (hours) medium (g.) agent (g.)

77 vinylace- 7 21 water hydroxymethyltate 0.7 (250) cellulose mole/pro- (0.55)

pylenc 1.49 mole 78 do. do. do. 24 do. do. 79* vinyl- 2.2 2% do. SINNOPON chloride (400) 'ADG( l) 1.6 mole/ (0.8) vinylace tate 1.16

mole I 80* do. 15 do. 18 do. do.

81 vinylace- 16.5 38 21 do. do.

tate 2.18 moles] ethylene 68 moles Example Oxidant Chelate Electron Degree of Viscosity Composition of copolymer (moles) (moles) donor conversion index in "/1 by weight (moles) 7) (em /g.) 77 2,4-dich1oro vanadyl NH OH 21 vinylacetate 87% benzoyl peracetylace- (1.2X10") propylene 13% oxide tonate (7.4X10) (3.7Xl0') 78 do. do. do.

(5X10) (2.5X10) (1.1 l0) 19 vinylacetate 86.5% propylene 13.5% 79' KBrO vanadyl tetrahydro- 83.5 130 (at vinylchloride 62.5% (2.5X10') acetylacefuran C in vinylacetate 37.5%

tonate (9.3X10) solution 1.25X10) ,at 5 g/l cyclohexanone) 80* do. do. do. 91 189 vinylchloride 62.5% (6.2 l0 (3.1X10) (2.3X10 vinylacetate 37.5% 81* do. do. do. 33.5 78 in vinylacetate 73% (5 l0 (2.5X10') (4X10"") toluene ethylene 27% experiment conducted in the presence of 0.67 g. of NaHCO to buffer the medium experiment conducted in the presence of 1.26 g. of NaHCO, to buffer the medium (1) SlNNOPON ASD sodium dndecylbenzene-sulphonate. I

EXAMPLE 82 EXAMPLE 84 Lauroyl peroxide (0.1 mol.), vanadyl acetylacetonate (0.1 mol.), Nl-l OH (0.44 mol.), methanol (10 l. vinyl chloride (64 mol., 4,000 g.), and ethylene (53 mol. 1,490 g.) are introduced into a 25-litre stainless steel autoclave. The pressure in the autoclave is 18 bars. The temperature is maintained at 16C for 21 hours with stirring. 2,200 g. of copolymer comprising 91.5 percent by weight of vinyl chloride and 8.5 percent by weight of ethylene are obtained. The degree of conversion is percent. The viscosity of the copolymer, measured on a solution having a concentration of 5 g/l. in a mixture of monochlorobenzene and cyclohexanone (50/50) at 25C, is 74 em /g.

EXAMPLE 83 A 3.6-litre stainless-steel autoclave equipped with a stirrer consisting of a frame rotating at 240 rpm, with tylacetonate (5.2 g., 0.0196 mol.) an aqueous NH O1-1 solution (d= 0.926, 4 cc., i.e., 0.0474 mol.), and finally ethylene to a pressure of 50 bars. Stirring is continued for 18 hours at 17C. After releasing the residual ethylene, 31 g. of a white powder shown to be polyethylene in infra-red spectrography are obtained. The melting point determined bydifferentialthermal analysis is EXAMPLE 85 The procedure of Example 84 is adopted, the methanolbeing replaced by cyclohexane'(l,020 g.) and the ammonia by n-butylamine' (4.3 cc., 0.0435v mol.), and the ethylene being introduced to a pressure of 45 bars.

65 After 6 hours at 17C, 50 g. of polyethylene, mp.

C, are obtained.

1 claim: 1. l roce s s fo'r the ptgytnerization of an olefinic monomer selected from the group consisting of a vinyl chloride, a vinylidene chloride, ethylene, propylene, a mixture of said monomers, and a mixture of said monomer with a vinyl ester which comprises contacting said monomer, at a temperature from 30 to +100C, with a polymerization initiator consisting essentially of a combination of (I) an oxidizing agent selected from the group consisting of hydrogen peroxide, persulphates, permanganates, chlorates, perchlorates, bichromates, bromates, ceric salts, oxaziranes, and organic peroxides andhydroperoxides, (2) a chelate compound of a metal in which compound the metal is still capable of accepting one or more electron pairs from an electron donor, the said chelate compound having the formula:

in which X represents an anion or .a cation; n is zero, a

in the case of non-ionizable chelates, or an integer or an improper fraction, in the case ofionizable chelates, equal to the number of electrical charges of the ionic grouping M is titanium. iron, vanadium, aluminum, tin, manganese, chromium, cobalt, copper, zinc, or bismuth; Q is an oxygen or sulphur atom or a lower alkyl or lower alkoxy group: D is an electron doublet donor group selected from the group consisting of carbonyl, carboxyl, amino, imino, amido, hydroxy, and mercapto; A joins together the D radicals and either is a valence bond or a hydrocarbon chain of up to 12 carbon atoms carrying the groups D terminally or at any point on or in the chain, the said chain being linear or branched and unsubstituted or substituted by an aromatic or a cycloaliphatic residue or is a polyvalent cyclic aromatic residue, p is an integer equal to or higher than 2, which is the number of donor groups in the ligand of formula DpA, s is zero or an integer. and m is an integer equal to or higher than 1, s and m being such that pm s has a value lower than the maximum coordination number of the metal M, the ratio of the number of gram-atoms of M to the number of moles of oxidizing agent being equal to or greater than 0.24:1 and (3) an electron donor in amount at most equal to that required to complex completely the metal of the chelate compound, the said electron donor being selected from the group consisting of amines, alcohols. ethers, aldehydes, ketones, imines, oximes, amides, sulphonamides, and phosphonamides, the molar proportions of said components (1) and (2) of the said initiator being each 0.0005 to 5 percent based on the monomer.

2. Process'according to claim l in which the olefinic monomer is vinyl chloride, a mixture of vinyl chloride and vinyl acetate, ethylene, or a mixture thereof.

3. Process according to claim 1 in which the polymerization is effected at an absolute pressure of l to bars.

4. Process according to claim 1 in which the said chelate compound is vanadyl acetylacetonate, ferrous acctylacetonate, vanadyl methylacetylacetonate, vanadyl Z-acetylcyclohexanate, vanadyl heptanedionatc, vana- UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,860.5568 I Dated January 975 CHABERT ET AL.

Inventor(s) It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

IN THE READING:

Please delete the statement of the inventors in its entirety and substitute therefor the following statement of the inventors and their residencies.

--Inventors: Henri Chabert, Lyon; Robert Aime Chapurlat, Lyon; Claude Gigou, Vernaison (Rhone);

Michel Ruaud, Villeneuve Par Ternay (Isere), all of France--' Signed sealer? this 15thday of April 1575.

FORM 90-1050 (O-69) Q ll 5 GOVIINIU" IIINIIIM OHILI. "I! H ".0 HI 

2. Process according to claim 1 in which the olefinic monomer is vinyl chloride, a mixture of vinyl chloride and vinyl acetate, ethylene, or a mixture thereof.
 3. Process according to claim 1 in which the polymerization is effected at an absolute pressure of 1 to 100 bars.
 4. Process according to claim 1 in which the said chelate compound is vanadyl acetylacetonate, ferrous acetylacetonate, vanadyl methylacetylacetonate, vanadyl 2-acetylcyclohexanate, vanadyl heptanedionate, vanadyl propionyl acetaldehydate, vanadyl benzoyl acetaldehydate, dichloro-titanium acetylacetonate, diethyl-tin acetylacetonate, cupric acetylacetonate, vanadyl salicyaldehydate, vanadyl-bis(acetyl acetamide), vanadyl-bis(acetylacetanilide), vanadyl thioglycollate, vanadyl anthranilate, zinc acetylacetonate, ethoxy aluminum acetylacetonate, manganous acetylacetonate, titanylacetylacetonate, ethyl titanyl-bis(acetylacetonate), vanadyl 3-chloroacetylacetonate or vanadyl Alpha -formyl cyclohexanonate.
 5. Process according to claim 1 in which the olefinic monomer is vinyl chloride and the temperature of polymerization is 10* to 20*C. 